Lung Cancer Trial, Recruiting NCT07612722 Sponsor: Wen-zhao ZHONG Condition: Lung Cancer
Back to Lung Cancer

Lung Cancer Trial, Recruiting

NCT07612722
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are willing to take part and have signed a consent form agreeing to join the study
  • People aged 18 to 74 years old (any gender)
  • People whose general physical health is rated as fully active or able to carry out light work, based on a standard medical scoring system called ECOG (scores 0 or 1)
  • People whose doctors expect them to live for at least 12 months
  • People who have been confirmed by tissue testing to have a type of lung cancer called non-small cell lung cancer (NSCLC) that is located in the outer part of the lung, at a stage between IIA and IIIB (using IASLC 9th edition staging), and whose cancer does not have certain genetic changes known as EGFR mutations or ALK rearrangements
  • People whose cancer is contained within a single section (lobe) of the lung, with no solid tumours spread across different lobes
  • People who have not had open chest surgery on the same side of the chest before
  • People who have already completed 2 to 4 cycles of pre-surgery treatment (called neoadjuvant therapy) involving both an immunotherapy drug (a PD-1 or PD-L1 inhibitor) and a two-drug platinum-based chemotherapy combination
  • People whose heart and lung function is considered sufficient for surgery, including specific breathing test results (FEV1 of at least 1.5 L or a lung gas exchange measure called DLCO of at least 40%), as assessed by the treating doctor
  • People whose tumour is more than 2 cm away from the airway opening, based on a pre-surgery CT scan
  • People whose tumour has been assessed by a review committee as suitable for a specific type of lung surgery that removes less than a full lobe, while completely removing the cancer (called sub-lobe R0 resection)

Who may not be able to join:

  • People who are not expected to tolerate a full lobe removal surgery (lobectomy)
  • People who have received radiation therapy to the chest before the planned surgery
  • People who have had a transplant of donated tissue or a solid organ (such as a kidney or liver)
  • People who have been diagnosed with an autoimmune disease, or who have been taking steroid medication (such as prednisone at more than 10 mg per day) or other immune-suppressing treatments within the 3 months before surgery
  • People who have a history of a non-infectious lung scarring condition (interstitial lung disease) that has required steroid treatment, or who currently have this condition and need steroid treatment for it
  • People who test positive for HIV, or who have active hepatitis B or active hepatitis C, based on blood tests done during the screening period
  • People with high blood pressure that is not well controlled by medication, meaning blood pressure readings remain above 150/90 mmHg on average across the three most recent measurements taken before joining the study
  • People who have an active infection during the screening period that still requires intravenous (drip) antibiotic or antiviral treatment
  • People who have had another cancer (other than certain low-risk or fully treated cancers such as skin basal cell cancer, cervical or breast cancer in situ, superficial bladder cancer, or localised prostate cancer) within the 3 years before signing the consent form — though people with low-risk early prostate cancer under stable active monitoring or who have received curative treatment may still be considered eligible (confirm with trial site)
  • People whose situation, in the treating doctor's judgement, could interfere with the study results or for whom participation would not be in their best interest
  • People who are pregnant, breastfeeding, or planning to become pregnant, or who have a positive pregnancy blood test within 7 days before starting the study treatment
  • People who are unlikely to follow the study procedures or are unwilling or unable to complete the full study process

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +8616620072467

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Wen-zhao ZHONG
Registry
ClinicalTrials.gov
Start date
18 May 2026
Est. completion
31 May 2034

Where this trial is recruiting

🇨🇳 China

Primary endpoints

3y-DFS

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov